ClinVar Miner

List of variants in gene MMP9 reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004994.3(MMP9):c.773C>T (p.Thr258Ile)	rs41529445	0.00148
NM_004994.3(MMP9):c.1468_1491del (p.Ser490_Pro497del)	rs761086664

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